CD 163
CD163 is a transmembrane protein mediating the endocytosis of haptoglobin-haemoglobin complexes. It is expressed on chromosome 12p13.3 and is a member of the cysteine-rich scavenger receptor superfamily. It is highly expressed by tissue macrophages and to a lesser extent by circulating monocytes. In a soluble form in plasma, it has an anti-inflammatory function. Expression is upregulated in inflamed tissues under the regulation of glucocorticoids, IL-10 and other modulators.
Immunohistochemical expression
CD163 shows a greater specificity for both non-neoplastic cells and tumours of monocyte/macrophage lineage than does CD681.
On flow cytometry, expression of CD163 in AML is largely restricted to FAB type
M5(16 of 19 cases) and to a lesser extent
M4(3 of 12 cases), other subtypes being negative (41 of 47 cases) or showing staining of less than 10% of cells (6 of 47 cases)17.
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CD163
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CD68
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Haematolymphoid diseases
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AML FAB M5
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2/61
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11/11(FAB M4 or M5)2
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AML other than FAB M5
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0/161
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2/18FAB other than M4 or M5)2
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Mast cell leukaemia
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0/11
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Lymphomas
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0/70(11 Angioimmunoblastic T cell, 1 Burkitt's, 2 CLL/SLL, 12 DLBCL, 27 follicular lymphomas, 2 lymphoplasmacytic, 6 marginal zone, 1 myeloma, 3 peripheral T cell, 1 precursor T cell, 2 PTLD)1
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16% of 4215,11
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Follicular dendritic cell tumour
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0/41
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6/133
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Haemophagocytic lymphohistiocytosis
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4/41
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Histiocytic sarcoma
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3/41
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26/263,4,5, 14/1416
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Langerhans cell histiocytosis
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3/51
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14/173
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Littoral cell angioma
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6/61
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6/66
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Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfmann disease)
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5/61
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20/2015
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Mesenchymal neoplasms
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Benign fibrous histiocytoma
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6/91
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4/45
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Atypical fibrous histiocytoma
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9/161
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Epithelioid histiocytoma
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1/11
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Giant cell tumour (tenosynovial)
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7/8(positivity in the epithelioid cell, negativity in osteoclast-like giant cells)1,
5/5(strong positivity in the small histiocytic cells, variable reactivity in plump mononuclear cells and negativity in osteoclast-like giant cells)8
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4/48
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Atypical fibroxanthoma
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1/31
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21/377
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DFSP
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1/4(in the positive case, staining was limited to less than 10% of tumour cells)1
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1/15
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Juvenile xanthogranuloma
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1/11
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Atypical lipomatous tumour
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2/24(in the positive cases, staining was limited to less than 10% of tumour cells)1
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Leiomyosarcoma
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1/33(in the positive case, staining was limited to less than 10% of tumour cells)1
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MFH
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2/53(in the positive cases, staining was limited to less than 10% of tumour cells)1
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42/715,13,14
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SFT
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1/9(in the positive case, staining was limited to less than 10% of tumour cells)1
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Alveolar soft part sarcoma
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0/21
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Angiosarcoma
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0/71
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2/46
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Carcinosarcoma
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0/71
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Myxoid chondrosarcoma
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0/21
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Clear cell sarcoma
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0/21
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Dermoid cyst
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0/11
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DSRCT
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0/31
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Elastofibroma
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0/11
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Endometrial stromal sarcoma
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0/61
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Epithelioid sarcoma
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0/11
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Ewing's sarcoma
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0/21
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Fibromatosis
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0/141
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Fibromyxoid sarcoma
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0/11
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Fibrosarcoma
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0/31
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Ganglioneuroma
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0/11
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GIST
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0/381
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Glomus tumour
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0/41
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Granular cell tumour
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0/21
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20/215,9,10
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Haemangioendothelioma
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0/31
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Haemangioma
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0/31
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5/106
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Haemangiopericytoma
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0/11
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Hibernoma
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0/11
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Inflammatory pseudotumour
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0/21
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Kaposi's sarcoma
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0/21
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Leiomyoma
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0/91
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Lipoblastomatosis
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0/41
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Lymphangioma
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0/11
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MPNST
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0/151
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Myofibrosarcoma
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0/21
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Myxoma
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0/11
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Myxosarcoma
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0/11
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Neurofibroma
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0/21
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18/185,9
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Nodular fasciitis
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0/21
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Osteosarcoma
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0/71
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Rhabdomyosarcoma
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0/111
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Sarcoma, NOS
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0/71
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Schwannoma
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0/31
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21/265,9
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Synovial sarcoma
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0/141
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Non-haematolymphoid, non-mesenchymal tumours
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Adrenal
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0/8(3 adenomas, 1 neuroblastoma, 4 phaeochromocytomas)1
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Bladder
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0/22(21 transitional cell carcinomas, 1 phaeochromocytoma)1
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Breast
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0/14(8 adenomas/papillomas, 6 ductal carcinomas)1
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Cervix
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0/8(8 carcinomas)1
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Colon
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0/95(87 adenocarcinomas, 4 adenomas, 2 carcinoids, 2 squamous cell carcinomas)1
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ENT
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0/30(29 squamous cell carcinomas, 1 low grade tumour)1
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Gallbladder
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0/1(1 cholangiocarcinoma)1
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Kidney
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0/44(34 renal cell carcinomas, 5 transitional cell carcinomas, 3 Wilm's tumours, 1 nephroma, 1 oncocytoma)1
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Liver
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0/18(14 hepatocellular carcinomas, 2 carcinoids, 1 cholangiocarcinoma, 1 hepatoblastoma)1
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Lung
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0/54(52 carcinomas, 2 neuroendocrine tumours)1
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Ovary
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0/46(28 serous, 10 adenocarcinomas, 6 clear cell, 1 mucinous, 1 seminoma)1
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Malignant melanoma
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0/221
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31/565,12
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Oesophagus
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0/16(8 squamous, 7 adenocarcinomas)1
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Pancreas
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0/12(9 adenocarcinomas, 1 adenoma, 1 islet cell tumour, 1 anaplastic)1
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Pleura
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0/4(mesotheliomas)1
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Prostate
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0/34(34 carcinomas)1
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Skin,BCC
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0/11
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Stomach
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0/26(26 adenocarcinomas)1
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Testis
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0/12(11 seminomas, 1 malignant mixed tumour)1
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Thymus
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0/1(thymoma)1
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Thyroid
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0/17(16 papillary, 1 follicular)1
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Uterus
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0/31(26 endometrioid, 4 clear cell, 1 mixed Mullerian tumour)1
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Vulva
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0/2(1 squamous cell carcinoma, 1 Paget's disease)1
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Diagnostic utility
Identification of entities of monocyte/macrophage differentiation.
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Differentiation of synovial macrophages (positive) from synovial fibroblasts (negative): both cell types are positive for CD68.
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Splenic littoral cell angioma (positive) from reactive splenic proliferations (negative)1.
References
1 Nguyen TT, Schwartz EJ, West RB, et al. Expression of CD163 (hemoglobin scavenger receptor) in normal tissues, lymphomas, carcinomas, and sarcomas is largely restricted to the monocyte/macrophage lineage. Am J Surg Pathol 2005; 29:617-24
2 Davey FR, Erber WN, Gatter KC, et al. The use of monoclonal antibody Y1/82A in the identification of acute myeloblastic and monocytic leukemias. Am J Clin Pathol 1988; 89:76-80
3 Pileri SA, Grogan TM, Harris NL, et al. Tumours of histiocytes and accessory dendritic cells: an immunohistochemical approach to classification from the International Lymphoma Study Group based on 61 cases. Histopathology 2002; 41:1-29
4 Hanson CA, Jaszcz W, Kersey JH, et al. True histiocytic lymphoma: histopathologic, immunophenotypic and genotypic analysis. Br J Haematol 1989; 73:187-98
5 Gloghini A, Volpe R, Canzonieri V, et al. Immunohistochemical characterization of Ki-M6 monoclonal antibody in Bouin-fixed, paraffin-embedded sections of normal and neoplastic human tissues. Virchows Arch A Pathol Anat Histopathol 1991; 418:355-60
6 Arber DA, Strickler JG, Chen YY, et al. Splenic vascular tumors: a histologic, immunophenotypic, and virologic study. Am J Surg Pathol 1997; 21:827-35
7 Longacre TA, Smoller BR,Rouse RV. Atypical fibroxanthoma. Multiple immunohistologic profiles. Am J Surg Pathol 1993; 17:1199-209
8 Furlong MA, Motamedi K, Laskin WB, et al. Synovial-type giant cell tumors of the vertebral column: a clinicopathologic study of 15 cases, with a review of the literature and discussion of the differential diagnosis. Hum Pathol 2003; 34:670-9
9 Tos AP, Doglioni C, Laurino L, et al. KP1 (CD68) expression in benign neural tumours. Further evidence of its low specificity as a histiocytic/myeloid marker. Histopathology 1993; 23:185-7
10 Tsang WY,Chan JK. KP1 (CD68) staining of granular cell neoplasms: is KP1 a marker for lysosomes rather than the histiocytic lineage? Histopathology 1992; 21:84-6
11 Carbone A, Gloghini A, Volpe R, et al. KP1 (CD68)-positive large cell lymphomas: a histopathologic and immunophenotypic characterization of 12 cases. Hum Pathol 1993; 24:886-96
12 Facchetti F, Bertalot G,Grigolato. PG KP1 (CD 68) staining of malignant melanomas. Histopathology 1991; 19:141-5
13 Binder SW, Said JW, Shintaku IP, et al. A histiocyte-specific marker in the diagnosis of malignant fibrous histiocytoma. Use of monoclonal antibody KP-1 (CD68). Am J Clin Pathol 1992; 97:759-63
14 Smith ME, Costa MJ,Weiss SW. Evaluation of CD68 and other histiocytic antigens in angiomatoid malignant fibrous histiocytoma. Am J Surg Pathol 1991; 15:757-63
15 Eisen RN, Buckley PJ,Rosai J. Immunophenotypic characterization of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease). Semin Diagn Pathol 1990; 7:74-82
16 Hornick, J. L., E. S. Jaffe, et al. (2004). "Extranodal histiocytic sarcoma: clinicopathologic analysis of 14 cases of a rare epithelioid malignancy." Am J Surg Pathol 28(9): 1133-44.
17 Walter RB, Bachli EB, Schaer DJ, et al. Expression of the hemoglobin scavenger receptor (CD163/HbSR) as immunophenotypic marker of monocytic lineage in acute myeloid leukemia. Blood 2003; 101:3755-6
This page last revised 30.6.2005.
©SMUHT/PW Bishop